Caleb Ibitamuno, Erlitz Luca, Telek Vivien, Vecsernyés Mónika, Sétáló György, Hardi Péter, Takács Ildikó, Jancsó Gábor, Nagy Tibor
Institute of Surgical Research and Techniques, University of Pécs Medical School, 7624 Pécs, Hungary.
Central Electron Microscope Laboratory, Institute of Medical Biology, University of Pécs Medical School, 7624 Pécs, Hungary.
Metabolites. 2021 Jun 17;11(6):396. doi: 10.3390/metabo11060396.
Cold ischemic injury to the intestine during preservation remains an unresolved issue in transplantation medicine. Autophagy, a cytoplasmic protein degradation pathway, is essential for metabolic adaptation to starvation, hypoxia, and ischemia. It has been implicated in the cold ischemia (CI) of other transplantable organs. This study determines the changes in intestinal autophagy evoked by cold storage and explores the effects of autophagy on ischemic grafts. Cold preservation was simulated by placing the small intestines of Wistar rats in an IGL-1 (Institute George Lopez) solution at 4 °C for varying periods (3, 6, 9, and 12 h). The extent of graft preservation injury (mucosal and cellular injury) and changes in autophagy were measured after each CI time. Subsequently, we determined the differences in apoptosis and preservation injury after activating autophagy with rapamycin or inhibiting it with 3-methyladenine. The results revealed that ischemic injury and autophagy were induced by cold storage. Autophagy peaked at 3 h and subsequently declined. After 12 h of storage, autophagic expression was reduced significantly. Additionally, enhanced intestinal autophagy by rapamycin was associated with less tissue, cellular, and apoptotic damage during and after the 12-h long preservation. After reperfusion, grafts with enhanced autophagy still presented with less injury. Inhibiting autophagy exhibited the opposite trend. These findings demonstrate intestinal autophagy changes in cold preservation. Furthermore, enhanced autophagy was protective against cold ischemia-reperfusion damage of the small bowels.
在移植医学中,肠道在保存过程中的冷缺血损伤仍是一个未解决的问题。自噬是一种细胞质蛋白降解途径,对于代谢适应饥饿、缺氧和缺血至关重要。它与其他可移植器官的冷缺血(CI)有关。本研究确定了冷藏引起的肠道自噬变化,并探讨了自噬对缺血移植物的影响。通过将Wistar大鼠的小肠置于4℃的IGL-1(乔治·洛佩兹研究所)溶液中不同时间(3、6、9和12小时)来模拟冷藏。在每个冷缺血时间后测量移植物保存损伤程度(黏膜和细胞损伤)以及自噬变化。随后,我们确定了用雷帕霉素激活自噬或用3-甲基腺嘌呤抑制自噬后凋亡和保存损伤的差异。结果显示,冷藏诱导了缺血损伤和自噬。自噬在3小时达到峰值,随后下降。储存12小时后,自噬表达显著降低。此外,雷帕霉素增强肠道自噬与12小时长时间保存期间及之后较少的组织、细胞和凋亡损伤相关。再灌注后,自噬增强的移植物损伤仍然较少。抑制自噬则呈现相反趋势。这些发现证明了冷保存过程中肠道自噬的变化。此外,增强自噬对小肠冷缺血-再灌注损伤具有保护作用。